m-Chloroperbenzoic acid → HCID 22618454, compound

HRID 1078464Notes

Reaction equation

HRID 1078464 reaction equation
[NH2:1][C:2]1[N:6]([C:7]2[C:12]([Cl:13])=[CH:11][C:10]([C:14]([F:17])([F:16])[F:15])=[CH:9][C:8]=2[Cl:18])[N:5]=[C:4]([C:19]([F:22])([F:21])[F:20])[C:3]=1[S:23][CH3:24].ClC1C=CC=C(C(OO)=[O:33])C=1>C(Cl)(Cl)Cl.ClCCl>[NH2:1][C:2]1[N:6]([C:7]2[C:12]([Cl:13])=[CH:11][C:10]([C:14]([F:15])([F:16])[F:17])=[CH:9][C:8]=2[Cl:18])[N:5]=[C:4]([C:19]([F:21])([F:20])[F:22])[C:3]=1[S:23]([CH3:24])=[O:33]

Participants

5

Procedure

A stirred solution of 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-methylthio-3-trifluoromethylpyrazole (1.0 g) in chloroform (40 ml) was treated with m-chloroperbenzoic acid (0.42 g), portionwise at room temperature. After stirring for 6 hours, the solution was diluted with dichloromethane and washed in turn with sodium sulphite solution, sodium hydroxide solution, and water. The solution was dried over anhydrous magnesium sulphate, and evaporated in vacuo to give a yellow oil. Purification by chromatography on silica (Merck 230-400 mesh, 0.7 kg cm-2) eluting with dichloromethane-ethylacetate (4:1) gave 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-methylsulphinyl-3-trifluoromethylpyrazole in the form of a white solid, m.p. 142°-145° C. with decomposition.

Workup

  1. washwashed in turn with sodium sulphite solution, sodium hydroxide solution, and water
  2. dry with materialThe solution was dried over anhydrous magnesium sulphate
  3. customevaporated in vacuo
  4. customto give a yellow oil
  5. customPurification by chromatography on silica (Merck 230-400 mesh, 0.7 kg cm-2)
  6. washeluting with dichloromethane-ethylacetate (4:1)

Sources & evidence

ORD record
ord-8f0bc7a4171440f6b0b205349ee51831
Source dataset
uspto-grants-1996_08
Patent number
US05547974

Reaction notes

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